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Journal Abstract Search

457 related items for PubMed ID: 28000143

  • 21. Detection of Novel Mutation in Ccm3 Causes Familial Cerebral Cavernous Malformations.
    Scimone C, Bramanti P, Ruggeri A, Katsarou Z, Donato L, Sidoti A, D'Angelo R.
    J Mol Neurosci; 2015 Nov; 57(3):400-3. PubMed ID: 26115622
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  • 22. Identification of a c.601C>G mutation in the CCM1 gene in a kindred with multiple skin, spinal and cerebral cavernous malformations.
    Haghighi A, Fathi D, Shahbazi M, Motahari MM, Friedman B.
    J Neurol Sci; 2013 Nov 15; 334(1-2):97-101. PubMed ID: 24007869
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  • 23. Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.
    Battistini S, Rocchi R, Cerase A, Citterio A, Tassi L, Lando G, Patrosso MC, Galli R, Brunori P, Sgrò DL, Pitillo G, Lo Russo G, Marocchi A, Penco S.
    Arch Neurol; 2007 Jun 15; 64(6):843-8. PubMed ID: 17562932
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  • 24. Deletions in CCM2 are a common cause of cerebral cavernous malformations.
    Liquori CL, Berg MJ, Squitieri F, Leedom TP, Ptacek L, Johnson EW, Marchuk DA.
    Am J Hum Genet; 2007 Jan 15; 80(1):69-75. PubMed ID: 17160895
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  • 25. Molecular diagnosis in cerebral cavernous malformations.
    Mondejar R, Lucas M.
    Neurologia; 2017 Oct 15; 32(8):540-545. PubMed ID: 26304651
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  • 26. Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI.
    Dammann P, Wrede K, Zhu Y, Matsushige T, Maderwald S, Umutlu L, Quick HH, Hehr U, Rath M, Ladd ME, Felbor U, Sure U.
    J Neurosurg; 2017 Feb 15; 126(2):570-577. PubMed ID: 27153162
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  • 31. A Novel KRIT1/CCM1 Gene Insertion Mutation Associated with Cerebral Cavernous Malformations in a Chinese Family.
    Wang H, Pan Y, Zhang Z, Li X, Xu Z, Suo Y, Li W, Wang Y.
    J Mol Neurosci; 2017 Feb 15; 61(2):221-226. PubMed ID: 28160210
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  • 33. Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.
    Gianfrancesco F, Cannella M, Martino T, Maglione V, Esposito T, Innocenzi G, Vitale E, Liquori CL, Marchuk DA, Squitieri F.
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jul 05; 144B(5):691-5. PubMed ID: 17440989
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  • 34. Spectrum of genotype and clinical manifestations in cerebral cavernous malformations.
    Gault J, Sain S, Hu LJ, Awad IA.
    Neurosurgery; 2006 Dec 05; 59(6):1278-84; discussion 1284-5. PubMed ID: 17277691
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  • 35. Cerebral cavernous malformations: from CCM genes to endothelial cell homeostasis.
    Fischer A, Zalvide J, Faurobert E, Albiges-Rizo C, Tournier-Lasserve E.
    Trends Mol Med; 2013 May 05; 19(5):302-8. PubMed ID: 23506982
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  • 37. Clinical features of cerebral cavernous malformations patients with KRIT1 mutations.
    Denier C, Labauge P, Brunereau L, Cavé-Riant F, Marchelli F, Arnoult M, Cecillon M, Maciazek J, Joutel A, Tournier-Lasserve E, Sociéte Française de Neurochirgurgie, Sociéte de Neurochirurgie de Langue Française.
    Ann Neurol; 2004 Feb 05; 55(2):213-20. PubMed ID: 14755725
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  • 38. A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas.
    Cigoli MS, De Benedetti S, Marocchi A, Bacigaluppi S, Primignani P, Gesu G, Citterio A, Tassi L, Mecarelli O, Pulitano P, Penco S.
    J Mol Neurosci; 2015 Jul 05; 56(3):602-7. PubMed ID: 25869611
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  • 39. Structural basis for the disruption of the cerebral cavernous malformations 2 (CCM2) interaction with Krev interaction trapped 1 (KRIT1) by disease-associated mutations.
    Fisher OS, Liu W, Zhang R, Stiegler AL, Ghedia S, Weber JL, Boggon TJ.
    J Biol Chem; 2015 Jan 30; 290(5):2842-53. PubMed ID: 25525273
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  • 40. CCM3 mutations are uncommon in cerebral cavernous malformations.
    Verlaan DJ, Roussel J, Laurent SB, Elger CE, Siegel AM, Rouleau GA.
    Neurology; 2005 Dec 27; 65(12):1982-3. PubMed ID: 16380626
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